Recalls
Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.
Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.
The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.
Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.
Minimum severity
Nidek Medical is recalling 335 MARK5 NUVO 8 oxygen concentrators because a capacitor failure may cause a fire and loss of supplemental oxygen.
The FDA is recalling specific lots of Covidien ROTICULATOR 30-3.5 Single Use Staplers because the sterility barrier may be compromised, potentially affecting surgical safety.
Nidek Medical is recalling 3,638 NUVO LITE oxygen concentrators because a capacitor failure may cause a fire and loss of supplemental oxygen.
Nidek Medical is recalling 14,585 NUVO LITE oxygen concentrators worldwide because a capacitor failure could cause a fire or loss of supplemental oxygen.
The FDA is recalling 13,531 units of the Covidien ROTICULATOR 55-4.8 Single Use Stapler because the sterility barrier may be compromised.
Nidek Medical is recalling 82 MARK5 NUVO 8 STD oxygen concentrators because a capacitor failure may cause a fire and loss of supplemental oxygen.
Arrow International is recalling 1,085 units of 7FR 3-Lumen Arrowg+ard Blue Plus Central Venous Catheters due to potential voids in the catheter hub that could cause interlumen crossover.
GE Healthcare is recalling eight Aestiva 7900 anesthesia machines because a missing interlock slide may allow two vaporizers to deliver agents simultaneously.
Nidek Medical is recalling NUVO LITE oxygen concentrators because a capacitor failure may cause a fire and loss of supplemental oxygen.
Nidek Medical is recalling M5C5/Mark5 Nuvo/OCSI oxygen concentrators because a capacitor failure may cause a fire and loss of supplemental oxygen.
Nidek Medical is recalling 7,889 oxygen concentrators because a capacitor failure may cause a fire and loss of supplemental oxygen.
Nidek Medical is recalling MARK5 NUVO oxygen concentrators because a capacitor failure could cause a fire and stop oxygen supply.
The FDA is recalling specific lots of Covidien ROTICULATOR 55-3.5 Single Use Staplers because the sterility barrier may be compromised, posing a risk of infection during surgery.